369624-76-0

Basic information

• Product Name: 2-Oxazolidinone, 3-(2-bromo-3-methyl-1-oxobutyl)-4-phenyl-, (4R)-
• CAS NO: 369624-76-0
• Molecular Formula: C14H16BrNO3
• Molecular Weight: 326.19
• Mol File: 369624-76-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-Oxazolidinone, 3-(2-bromo-3-methyl-1-oxobutyl)-4-phenyl-, (4R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Oxazolidinone, 3-(2-bromo-3-methyl-1-oxobutyl)-4-phenyl-, (4R)-(369624-76-0)
• EPA Substance Registry System: 2-Oxazolidinone, 3-(2-bromo-3-methyl-1-oxobutyl)-4-phenyl-, (4R)-(369624-76-0)

Safety Data

• Hazardous Substances Data: 369624-76-0(Hazardous Substances Data)

Upstream product

• 26464-05-1 2-bromo-3-methyl-butyryl bromide 
• 90319-52-1 (4R)-phenyl-2-oxazolidinone 

Downstream Products

• 369624-75-9 (4'R)-2-bromo-1-(2'-oxo-4'-phenyloxazolidin-3'-yl)butan-1-one 
• 201300-96-1 (4'R)-2-bromo-1-(2'-oxo-4'-phenyloxazolidin-3'-yl)propan-1-one 
• 90319-52-1 (4R)-phenyl-2-oxazolidinone 

Relevant articles and documents

Stereoselective dimerization of chiral α-bromoamides promoted by Fe(Co)5

Organic α-bromocarboxylates react with aldehydes and ketones in the presence of Fe(CO)5 (the Reformatsky-type reactions). Unlike them, N-oxazolidinone derivatives of the same acids undergo diastereoselective reductive dimerization to give (2S,3S)-dimers, regardless of the configuration of the α-chiral center in the starting reagent.